BEUDAMED
    25 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    MULTICHEM U

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    AURORA SR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VIPER SYSTEM, EXPEDIUM SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SILTEX SALINE MAMMARY IMPLANT

    FDA Adverse Event
    Injury ·MENTOR·Product code FWM·May 18, 1998

    MEDTRONIC

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·April 24, 1998

    ZYPLAST COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·COLLAGEN CORP.·Product code LMH·April 22, 1997

    QUEST INFUSOR

    FDA Adverse Event
    Malfunction ·KENDALL MCGAW LABORATORY·Product code KZD·July 12, 1993

    ACUFEX TRAIL BLAZER (WITH NNULATED0 ( PROTOTYPE)

    FDA Adverse Event
    ACUFEX MICROSURGICAL, INC.·August 2, 1993

    HOYER LIFTER

    FDA Adverse Event
    Other ·JOERNS HEALTHCARE, INC.·Product code FSA·April 28, 2008

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    ENTRUST VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·June 16, 2011

    EEA XL 28MM SINGLE-USE STAPLER

    FDA Adverse Event
    Injury ·NORTH HAVEN-USS·Product code GDW·August 21, 2008

    ZIMMER SKIN GRAFT MESHER

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GFD·March 10, 2014

    IMPLANTED IN ANOTHER INSTITUTION.

    FDA Adverse Event
    Malfunction ·UNABLE TO DETERMINE ANY PERTINENT INFORMATION·April 28, 1993

    HOLMIUM: YAG 2.1. MICROMETER LASER

    FDA Adverse Event
    Malfunction ·TRIMEDYNE·Product code LXS·May 17, 1993

    CENTURY TUB (WHIRLPOOL) LIFT

    FDA Adverse Event
    Malfunction ·CENTURY MANUFACTURING CO.·Product code ILJ·February 8, 1993

    LP10 VOLUME VENTILATOR

    FDA Adverse Event
    Death ·AEQUITRON MEDICAL, INC.·Product code CBK·March 5, 1993

    GORE® DUALMESH® BIOMATERIAL

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code FTL·September 4, 2020

    INVACARE INNOVATION IN HEALTH CARE

    FDA Adverse Event
    Death ·INVACARE INNOVATION IN HEALTH CARE·August 31, 1993

    SUPER TORQUE

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DQO·August 25, 1993